Canonical Allele Identifier: CA2466663779
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379606T= , CM000685.2:g.154379606T= GRCh38
NC_000023.10:g.153607966T= , CM000685.1:g.153607966T= GRCh37
NC_000023.9:g.153261160T= NCBI36
NG_008677.1:g.10171T= , LRG_745:g.10171T=
NG_011506.1:g.41A=
NG_011506.2:g.33A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.82+40T= ENSP00000507245.1:n.82+40T=
ENST00000682478.1:n.58+40T=
ENST00000683576.1:n.58+40T=
ENST00000683627.1:c.82+40T= ENSP00000507533.1:n.82+40T=
ENST00000684082.1:c.82+40T= ENSP00000508266.1:n.82+40T=
ENST00000684633.1:n.54+44T=
ENST00000684678.1:c.78+44T= ENSP00000507059.1:n.78+44T=
ENST00000369842.9:c.82+40T= MANE Select ENSP00000358857.4:n.82+40T=
ENST00000369835.3:c.82+40T= ENSP00000358850.3:n.82+40T=
ENST00000369842.8:c.82+40T= ENSP00000358857.4:n.82+40T=
ENST00000428228.5:c.53+69T= ENSP00000401081.1:n.53+69T=
ENST00000468294.5:n.42+40T=
ENST00000485261.1:n.163+40T=
ENST00000486738.5:n.226+40T=
ENST00000494443.5:n.139+40T=
NM_000117.2:c.82+40T= , LRG_745t1:c.82+40T= NP_000108.1:n.82+40T=
XM_024452349.1:c.-127+40T= XP_024308117.1:n.-127+40T=
NM_000117.3:c.82+40T= MANE Select NP_000108.1:n.82+40T=